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Determination of Vitamin D Levels in Patients With Neurofibromatosis Type 1 in the Pediatric Age Group
Alessandra Santos1, Mauro Geller1,2,3, Spyros Mezitis4
1Department of Medical Genetics, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Insights
Vitamin D levels in children with Neurofibromatosis type 1 (NF1) did not correlate with gender, age, or neurofibroma count. Adequate sun exposure was linked to sufficient vitamin D levels in NF1 patients.
Area of Science:
- Genetics
- Pediatrics
- Endocrinology
Background:
- Neurofibromatosis type 1 (NF1) is a common genetic disorder with varied clinical manifestations.
- Skeletal issues and reduced bone mass are prevalent in NF1 patients.
- Previous studies noted low vitamin D in NF1 patients, but correlations in children remain unclear.
Purpose of the Study:
- To evaluate vitamin D levels in children and adolescents with NF1.
- To determine vitamin D levels across different age groups and explore correlations with age, gender, sun exposure, and neurofibroma presence.
Main Methods:
- An observational, cross-sectional study involving 55 NF1 patients.
- Vitamin D levels were measured using chemiluminescent immunoassay.
- Data were correlated with demographic factors, sun exposure, and neurofibroma characteristics.
Main Results:
- The mean vitamin D level was 30.82 ng/mL (median 29 ng/mL).
- Vitamin D levels did not significantly differ by gender, age group, or number of cutaneous neurofibromas.
- Sufficient vitamin D levels were more common in patients with adequate sun exposure.
Conclusions:
- Vitamin D levels in pediatric NF1 patients are not influenced by gender, age, or neurofibroma burden.
- Adequate sun exposure is associated with sufficient vitamin D levels in this population.
- Younger children (0-11 years) with NF1 showed a tendency towards vitamin D sufficiency compared to older adolescents (11-19 years).
Introduction:
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders. Some clinical manifestations are present at birth, while some develop during childhood, and others can occur at any age. Given the early age at which patients develop clinical features, diagnosis is often made during childhood. The most prevalent features of NF1 are café au lait spots, dermal and plexiform neurofibromas, and learning disability. A variety of skeletal problems may be seen in NF1, including scoliosis, short stature, and pseudoarthrosis. Reduced skeletal bone mass has been documented to be a common phenomenon in children and adults with NF1. Decreased serum 25-hydroxyvitamin D (vitamin D) levels have been noted in adults and children with NF1 and have been reported to be inversely correlated with the number of dermal neurofibromas in adults. However, the actual correlation of vitamin D level to bone density and dermal neurofibroma number in children with NF1 remains unclear.
Objectives:
The primary objective of this study was to evaluate vitamin D levels among children and adolescents with NF1. The secondary objective was to describe the levels of vitamin D among children and adolescents with NF1, to verify in which age group there is a higher frequency of vitamin D alterations, and to explore vitamin D level correlations between age, gender, sun exposure, number of neurofibromas, and number of plexiform neurofibromas.
Methods:
This was an observational, cross-sectional, hospital-based study. We obtained a convenience sample of individuals with confirmed diagnosis of NF1 from patients attending the Medical Genetics Service of the IPPMG-UFRJ and Santa Casa de Misericórdia of Rio de Janeiro over a 24-month period. We evaluated vitamin D levels in blood samples of patients with NF1 by a chemiluminescent immunoassay method, and we correlated the results with gender, age, number of neurofibromas, number of plexiform neurofibromas, and satisfactory sun exposure.
Results:
Of the 55 patients, 28 (50.9%) were female and 27 (49.1%) were male. Patient ages ranged from a minimum of 1.2 to a maximum of 19.6 years (mean age 10.95 years) and the median was 11.11 years. Median and mean body mass index (BMI; z score) were -0.09 (minimum value -1.63 and maximum of 4.62) and 0.16, respectively. The mean value of vitamin D was 30.82 ng/mL (±12.31) and the median was 29 ng/mL (minimum value of 10.40 ng/mL and maximum of 79.19 ng/mL).
Conclusions:
The levels of vitamin D did not differ according to gender, age group, or the presence or number of cutaneous neurofibromas. Among patients with adequate sun exposure, there was a higher incidence of sufficient serum vitamin D levels. Patients with cutaneous neurofibromas in the 0 to 11 age group had a greater tendency to vitamin D sufficiency in relation to patients aged 11 to 19 years.
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